Boron tribromide → HCID 22459006, compound
Reaction equation
[CH3:1][C:2]([CH3:16])([CH3:15])[CH2:3][C:4]1[C:8]2[CH:9]=[CH:10][C:11]([O:13]C)=[CH:12][C:7]=2[O:6][CH:5]=1.B(Br)(Br)Br>C(Cl)Cl>[CH3:1][C:2]([CH3:16])([CH3:15])[CH2:3][C:4]1[C:8]2[CH:9]=[CH:10][C:11]([OH:13])=[CH:12][C:7]=2[O:6][CH:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a −10° C. solution of the product of Step D (2.379 grams) in dry methylene chloride (35 mL) was added 1M boron tribromide solution (CH2Cl2; 3.70 mL). Warming to ambient temperature was followed by stirring for 1 hour. The reaction was partitioned between isopropyl acetate and aqueous sodium bicarbonate. The organic was washed twice with water and dried over magnesium sulfate. Filtration and removal of volatiles provided a residue which was chromatographed over silica gel (5:1 hex/ethyl acetate), giving the title compound.
Workup
- customThe reaction was partitioned between isopropyl acetate and aqueous sodium bicarbonate
- washThe organic was washed twice with water
- dry with materialdried over magnesium sulfate
- filtrationFiltration and removal of volatiles
- customprovided a residue which
- customwas chromatographed over silica gel (5:1 hex/ethyl acetate)
Sources & evidence
- ORD record
- ord-1a81473db01740c9b3a1a6406636a0c7
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06399640B1
Reaction notes
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